17284-06-9

Upstream product

• 22666-07-5 di-p-tolylbutadiyne 
• 538-28-3 S-benzylisothiourea hydrochloride 
• 100-53-8 phenylmethanethiol 
• 16212-89-8 (Z)-1-benzylthio-1,4-di(p-tolyl)-1-buten-3-yne 

Downstream Products

• 17284-11-6 (Z,Z)-1,4-di(p-tolyl)-1,3-butadiene-1,4-dithiol 
• 82366-98-1 2,5-bis(4'-methylphenyl)thiophene 
• 23460-42-6 Z,Z-1,4-Bis-(p-tolyl)-1,4-bis-(ethylmercapto)-buta-1,3-dien 
• 17284-15-0 (Z,Z)-1,4-di(acetylthio)-1,4-di(p-tolyl)-1,3-butadiene 
• 34102-87-9 3,6-bis(4-methylphenyl)pyridazine 
• 16212-86-5 3,6-di(p-tolyl)-1,2-dithiine 

Relevant academic research and scientific papers

1,2-Dithiines and precursors, XVI: Synthesis, structure, and reactivity of non-anellated 1,2-dithiines

Various monocyclic 1,2-dithiines 6a,b,d-t were prepared via (Z,Z)-1,4-difunctionalized butadienes (4-11,19,20). A twisted cyclic structure A is unequivocally proved rather than of the ringopened valence isomer B. The reactivity of these 1,2-dithiines is d